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- ...into TrackWise. The ideal candidate will bring an understanding of GMP principles, experience in pharmaceutical or dietary supplement... ...Documentation & Audit Support Collaborate with Document Control and QA teams to ensure controlled documents are accurate, current, and...SuggestedTemporary workWork at office
$65.99k - $90.74k
...seeking a Quality Assurance Associate Specialist in East Windsor Township, NJ. This role focuses on ensuring FDA compliance, reviewing GMP documentation, and releasing Finished Goods. The ideal candidate has a bachelor's degree in Engineering or Science and at least two...Suggested- ...focuses on change control of SOPs and batch records, preparation of GMP reports, and supporting FDA and ISO readiness while maintaining... ...have a bachelor’s degree in a scientific field and 2+ years in QA/QC, with experience in batch records and CAPA. #J-18808-Ljbffr...Suggested
- ...ideal candidate will have a Bachelor's degree in a scientific field and 3-5 years of relevant QA experience in a regulated environment. Responsibilities include conducting GMP investigations, managing quality metrics, providing hands-on training and support for FDA inspections...Suggested
- ...Binding Minds Inc. is seeking a quality professional in Boston with over 4 years of GMP experience in the pharmaceutical industry. The role involves quality oversight of external manufacturing and testing activities for clinical-stage products, requiring strong knowledge...Suggested
$156.6k - $234.8k
...Duties and Responsibilities Lead a Quality Operations team supporting GMP manufacturing/testing, including disposition of intermediates, working cell banks, and clinical/commercial drug products. Manage QA On the Floor and QA Walkthrough programs supporting Vertex GMP...SuggestedWork experience placementShift workDay shift$226.28k - $377.13k
...Responsibilities Lead a team of 5–7 MSMQs responsible for the independent QA function, with authority for final batch disposition, QA... ...manufacturing/testing, and independence from production per Daiichi Sankyo's GMP Quality Manuals. Resolve quality performance issues escalated...SuggestedContract workLocal area$122k - $150k
...backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and...SuggestedLocal areaFlexible hours3 days per week$156.6k - $234.8k
...Job Description General Summary The Associate Director, GMP Operational Quality is responsible for oversight of team activities, development... ...products internally at Vertex manufacturing facilities. Manages QA On The Floor and QA Walkthrough programs supporting Vertex GMP...SuggestedWork experience placementSummer workRemote workFlexible hoursDay shift2 days per week- ...activities, including testing and staff management. This role requires a Bachelor’s degree in Microbiology and 5+ years of experience in a GMP quality control environment. The ideal candidate will demonstrate strong leadership and problem-solving skills. The company offers...Suggested
$122k - $150k
...backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and...SuggestedLocal areaFlexible hours3 days per week- ...testing in a fast-paced pharmaceutical environment. You will perform critical quality checks and documentation to ensure compliance with GMP standards. Ideal candidates have a degree in a related field and 2-4 years of industry experience. This full-time position offers...SuggestedFull time
- ...A global pharmaceutical company located in Sacramento is seeking an In Process QA Specialist to ensure quality standards during manufacturing processes. Key responsibilities include real-time monitoring, testing, and documentation in line with Good Manufacturing Practices...Suggested
- ...REQUIREMENTS BS in chemistry, engineering, science, or equivalent experience Must have at least 3-5 years industrial experience in a GMP environment with good technical understanding of the GMP regulations and applications Application of GMPs have been demonstrated...SuggestedLocal areaNight shiftWeekend workDay shift
$25 - $34 per hour
...Merck & Co. is seeking a QA Inspector III in Hauppauge, NY, responsible for ensuring product quality during manufacturing and packaging processes. The role includes responsibilities such as monitoring raw materials, conducting in-process checks, and maintaining compliance...SuggestedHourly payFull time- ...A leading healthcare manufacturer is looking for a QA Inspector for the evening shift (3pm-11:30pm) in Shirley, NY. This role entails ensuring quality oversight in manufacturing processes, adhering to strict cGMP standards and conducting detailed inspections of products...Afternoon shift
$188k - $230k
...and communities. Learn more and follow us on X, LinkedIn and Facebook. Role Summary The Director of QA GMPOperations is responsible for management of GMP quality within our external manufacturing operations globally and internal GMP operations for development and...Local area$36 - $45 per hour
...assignment supporting quality and compliance activities within a GMP-regulated manufacturing environment. This hybrid position will provide... ...monitoring programs Cleanroom operations Provide QA oversight of aseptic processing activities to ensure compliance with...Contract workTemporary workLocal area2 days per week3 days per week$23.61 - $25 per hour
A pharmaceutical company based in Town of Brookhaven is seeking a Quality Assurance Inspector to provide oversight in manufacturing areas, ensuring compliance with quality programs and cGMP requirements. The role requires conducting product inspections, maintaining documentation...Hourly pay$55k - $65k
...appropriate, to support test planning, defect analysis, documentation, and release note drafting. Contribute to continuous improvement of QA processes, testing standards, documentation, and release readiness practices. Qualifications Required Education/Experience...Full timeWork at officeRemote work$30 - $35 per hour
...Job Title: QA Lead - Urgently Hiring Job Description The QA Lead oversees daily quality and laboratory operations within a... ...supplies, including laboratory testing chemicals, laboratory equipment, GMP/PPE materials (such as gloves, paper towels, hand soap), and...Contract workTemporary workLocal areaImmediate startShift work$138k - $190k
...Description Job Description We are seeking a Senior Manager, GMP Quality Assurance to support and continuously improve Quality... ...transfer, and qualification activities Mentor and develop junior QA staff Qualifications Qualifications ~ Bachelor’s degree...- Join to apply for the QA Analyst role at Boar's Head Brand 1 day ago Be among the first 25 applicants Join to apply for the QA Analyst... ...food safety. Also responsible for assigned area’s compliance to GMP’s, SQF requirements, QCCP verifications, HACCP verifications, SSOP...Full time
- ...determines solutions. Responsibilities The Quality Assurance (QA) Specialist will support a Quality Assurance Unit in the School of... ...report administratively to the Manager of Quality Assurance for GMP Operations. The QA Specialist will perform Quality Assurance activities...Flexible hours
- ...Job Description Job Description QA/RA Specialist - Pharmaceutical GLP/GMP Experience Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical...
- ...Job Description Job Description Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes...
- Position Overview The QA Engineer, DSM Operations is responsible to help drive the Quality oversight for the direction of all Drug Substance... ...of applicable experience • 3+ years of experience working in a GMP regulated environment • Experience in Validation, cGMP...Shift workDay shift
- ...implementing continuous improvement opportunities, and maintaining GMP compliance. Work Schedule: 2nd shift Sat - Wed 3/4pm - 11:30... ...let us know-we are happy to support you. Job Segment: QA Engineer, Medical Technologist, Quality Engineer, Nuclear Engineering...Work experience placementWork at officeShift workNight shiftAfternoon shift
- ...QA Supervisor Streetsboro Plastics Operations The Quality Assurance Supervisor leads daily quality operations and supports the site... ...accountable for quality execution, ISO 9001, AIB/Food Safety and GMP readiness, customer complaint response, CAPA effectiveness, audit...Temporary workRelocationFlexible hoursShift work
$73.7k - $110.5k
...Quality Assurance Supervisor, you will oversee the Quality Assurance (QA) team and programs for the Dixon, IL, site, a manufacturer of... ...Recalls, Food Safety Plans, and pest control systems. Conduct GMP and sanitation audits and summarize technical data to identify...Full timeWork at officeImmediate startShift workAfternoon shift

